HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877726Generated: November 1, 2026
Pentafluoropropionic acid → HCID 86643203, compound
https://huagongshe.com/reaction/1877726
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pentafluoropropionic acid | HCID 62356 | — |
| Reactant | HCID 15537423 | HCID 15537423 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | N-(2-Methoxyethyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamine | HCID 71424406 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86643203 | HCID 86643203 | — |
Reaction Steps
6.56 g (0.03 moles) of N,N-Bis(trimethylsilyl)-2-methoxyethylamine were mixed with 3.14 g (0.02 moles) of 4-(2-methoxyethylamino)-3-penten-2-one. To this mixture was added 4.1 g (0.026 moles) of pentafluoropropionic acid dropwise over 5 minutes with rapid stirring. The mixture darkened and became warm, eventually forming two immiscible layers, and was allowed to stir for 1 hour. 2.5 g (0.0266 moles) of sodium t-butoxide dissolved in 5 ml of tetrahydrofuran was then added dropwise over a five minute period. The mixture warmed and became one liquid phase, which was yellow. The solvent was then removed by vacuum distillation at room temperature, and the product then vacuum distilled out of the resulting residue as a clear liquid by heating>150° C. Yield of MeC(NCH2CHOMe)CHC(HNCH2CH2OMe)Me=3.9 g (91% of theoretical).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08313807B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-ae6bd8f3eb794bbbab8c8530435c4cb3 |
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| Source note | uspto-grants-2012_11 |
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